Search results for Sirolimus

1236 hits were found for Sirolimus

# Family MCID Name MIFTS Score
1
P CRN018 Coronary Artery Anomaly 63 0.350
2
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.344
3
ART140 Arteries, Anomalies of 53 0.326
4
P GRF003 Graft-Versus-Host Disease 71 0.296
5
P CRN300 Coronary Heart Disease 1 63 0.278
6
ISC004 Ischemia 60 0.264
7
P KDN018 Kidney Disease 70 0.249
8
c ACT135 Acute Graft Versus Host Disease 51 0.212
9
THR024 Thrombosis 56 0.202
10
P LKM002 Leukemia 66 0.199
11
HML018 Homologous Wasting Disease 22 0.196
12
LYM007 Lymphangioleiomyomatosis 68 0.186
13
P LYM118 Lymphoma 68 0.185
14
LYM019 Lymphosarcoma 47 0.180
15
CRN030 Coronary Stenosis 50 0.177
16
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.176
17
P TBR001 Tuberous Sclerosis 70 0.174
18
c ACT075 Acute Myocardial Infarction 56 0.174
19
P NTR004 Neutropenia 63 0.169
20
P LYM031 Lymphocytic Leukemia 55 0.166
21
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.161
22
c TBR025 Tuberous Sclerosis 1 76 0.159
23
ANG054 Angina Pectoris 66 0.159
24
END030 End Stage Renal Failure 58 0.158
25
c CHR417 Chronic Graft Versus Host Disease 56 0.158
26
DFC004 Deficiency Anemia 75 0.157
27
c HYP836 Hypercholesterolemia, Familial, 1 72 0.154
28
P MYC007 Myocardial Infarction 70 0.154
29
P MYL006 Myeloid Leukemia 60 0.154
30
MYL009 Myelodysplastic Syndrome 70 0.152
31
P LKM062 Leukemia, Acute Lymphoblastic 68 0.152
32
P THR014 Thrombocytopenia 68 0.149
33
SRC014 Sarcoma 65 0.149
34
SPN035 Spindle Cell Sarcoma 51 0.149
35
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.147
36
c LKM061 Leukemia, Acute Myeloid 83 0.144
37
HMT002 Hematologic Cancer 62 0.144
38
P HYP750 Hypertriglyceridemia, Familial 61 0.144
39
c PRM038 Primary Agammaglobulinemia 43 0.144
40
KPS004 Kaposi Sarcoma 75 0.141
41
THR123 Thrombotic Microangiopathy 38 0.140
42
INT007 Intermediate Coronary Syndrome 55 0.138
43
P HPT023 Hepatocellular Carcinoma 100 0.136
44
LYM133 Lymphoma, Hodgkin, Classic 69 0.134
45
LYM040 Lymphoblastic Lymphoma 54 0.134
46
P SKN015 Skin Carcinoma 67 0.133
47
c RHB024 Rhabdomyosarcoma 2 65 0.131
48
HMN016 Hemangioendothelioma 34 0.128
49
P HRT032 Heart Disease 75 0.127
50
48X005 48,xyyy 39 0.124
51
c LKM063 Leukemia, Chronic Myeloid 71 0.122
52
P DBT009 Diabetes Mellitus 64 0.122
53
P VSC007 Vascular Disease 63 0.122
54
CRN020 Coronary Restenosis 39 0.122
55
LPD008 Lipid Metabolism Disorder 62 0.120
56
SFT003 Soft Tissue Sarcoma 56 0.120
57
P PLY014 Polycystic Kidney Disease 59 0.119
58
c CHR064 Chronic Monocytic Leukemia 34 0.119
59
MYL069 Myeloma, Multiple 85 0.117
60
c LKM071 Leukemia, Chronic Lymphocytic 79 0.117
61
ADL002 Adult Syndrome 69 0.117
62
c CHR684 Chronic Kidney Disease 66 0.117
63
P EXN002 Exanthem 57 0.117
64
PLS009 Plasma Cell Neoplasm 51 0.117
65
KPS002 Kaposiform Hemangioendothelioma 43 0.117
66
c MLG074 Malignant Mesenchymoma 39 0.117
67
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.115
68
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.114
69
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.114
70
HYP056 Hypoglycemia 66 0.112
71
CYT008 Cytomegalovirus Infection 56 0.112
72
LYM022 Lymphangioma 53 0.112
73
ATX019 Ataxia with Vitamin E Deficiency 48 0.112
74
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.110
75
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.108
76
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.108
77
ATH013 Atherosclerosis Susceptibility 66 0.108
78
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.108
79
ALL026 Allergic Hypersensitivity Disease 64 0.107
80
LNG099 Lung Disease 61 0.107
81
P LYM033 Lymphoproliferative Syndrome 60 0.107
82
P BCL017 B-Cell Lymphoma 58 0.107
83
CYT002 Cytokine Deficiency 44 0.107
84
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.105
85
ATM095 Autoimmune Disease 61 0.103
86
MCS002 Mucositis 55 0.103
87
c TBR026 Tuberous Sclerosis 2 71 0.101
88
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.101
89
HYP066 Hyperglycemia 61 0.101
90
MNT001 Mantle Cell Lymphoma 66 0.099
91
P HMN010 Hemangioma 61 0.099
92
ANR040 Aneurysm 58 0.099
93
P UVT001 Uveitis 57 0.099
94
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.099
95
c HYP595 Hypertension, Essential 84 0.097
96
P TRN020 Turner Syndrome 65 0.097
97
DWN001 Down Syndrome 70 0.095
98
MYL005 Myelofibrosis 67 0.093
99
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.093
100
PST046 Post-Transplant Lymphoproliferative Disease 53 0.093
101
BRN002 Bronchiolitis 59 0.091
102
c ACT073 Acute Leukemia 58 0.091
103
P DRR001 Diarrhea 57 0.091
104
BRN012 Bronchiolitis Obliterans 56 0.091
105
STM007 Stomatitis 49 0.091
106
LYM005 Lymphocele 35 0.091
107
P LNG032 Lung Cancer 97 0.088
108
MYL031 Myeloproliferative Neoplasm 65 0.088
109
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 47 0.088
110
BNM001 Bone Marrow Cancer 43 0.088
112
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.086
113
P MCR115 Microvascular Complications of Diabetes 5 66 0.086
114
P KDN017 Kidney Cancer 61 0.086
115
ACR041 Acromelic Frontonasal Dysostosis 52 0.086
116
P RSP003 Respiratory Failure 74 0.084
117
P LYM025 Lymphedema 53 0.084
118
P SCK005 Sickle Cell Disease 50 0.084
119
ANG018 Angiomyolipoma 45 0.084
120
P NRF023 Neurofibromatosis, Type Ii 76 0.082
121
P CNR004 Cone-Rod Dystrophy 2 71 0.082
122
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.082
123
c ACT071 Acute Kidney Failure 59 0.082
124
P CHR285 Chronic Myelomonocytic Leukemia 59 0.082
125
c FML035 Familial Hyperlipidemia 55 0.082
126
P ART021 Arteriosclerosis 54 0.082
127
CRD137 Cardiogenic Shock 48 0.082
128
P CRN074 Coronary Artery Aneurysm 39 0.082
129
CRN006 Coronary Aneurysm 37 0.082
130
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.082
131
GLB015 Glioblastoma Multiforme 75 0.079
132
P APL001 Aplastic Anemia 74 0.079
133
P LVR013 Liver Disease 68 0.079
134
BRK010 Burkitt Lymphoma 67 0.079
135
P HPT021 Hepatitis 67 0.079
136
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.079
137
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.079
138
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.079
139
P NPH012 Nephrotic Syndrome 63 0.079
140
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.079
141
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.079
143
SCK003 Sickle Cell Anemia 72 0.077
144
P FLL037 Follicular Lymphoma 66 0.077
145
OST159 Osteogenic Sarcoma 66 0.077
146
NRF007 Neurofibroma 64 0.077
147
ART002 Arts Syndrome 63 0.077
148
EYD002 Eye Disease 58 0.077
149
IRN002 Iron Metabolism Disease 57 0.077
150
HYP005 Hypokalemia 55 0.077
151
c FLL041 Follicular Lymphoma 1 49 0.077
152
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.077
153
BLR027 Blue Rubber Bleb Nevus 40 0.077
154
SPR126 Superior Semicircular Canal Dehiscence 40 0.077
155
c HMG029 Hemoglobin Se Disease 38 0.077
156
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.074
157
c SYS001 Systemic Lupus Erythematosus 86 0.074
158
P GLM040 Glioma Susceptibility 1 81 0.074
159
CNG034 Congestive Heart Failure 70 0.074
160
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.074
161
c SML038 Small Cell Cancer of the Lung 65 0.074
162
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.074
163
LYM012 Lymphoplasmacytic Lymphoma 61 0.074
164
MRG003 Marginal Zone B-Cell Lymphoma 53 0.074
165
P PNV001 Panuveitis 51 0.074
166
P AST007 Astrocytoma 50 0.074
167
MCR004 Macroglobulinemia 50 0.074
168
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.074
169
P RRL003 Rare Lymphatic Malformation 31 0.074
170
P PRS040 Prostate Cancer 97 0.071
171
P PNC035 Pancreatic Cancer 84 0.071
172
PRP027 Peripheral Vascular Disease 71 0.071
173
P SRC025 Sarcoidosis 1 70 0.071
174
P PNM007 Pneumonia 68 0.071
175
c HPT001 Hepatitis C 63 0.071
176
P FCL005 Focal Segmental Glomerulosclerosis 58 0.071
177
P GLM007 Glomerulonephritis 57 0.071
178
HYP060 Hyperinsulinism 54 0.071
179
c MCR113 Microvascular Complications of Diabetes 3 52 0.071
180
VSC006 Vascular Cancer 51 0.071
181
P PRC012 Pericardial Effusion 51 0.071
182
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.071
183
SKN013 Skin Benign Neoplasm 49 0.071
184
HMP001 Hemopericardium 46 0.071
185
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.071
186
EWN003 Ewing Sarcoma 68 0.069
187
LVR012 Liver Cirrhosis 63 0.069
188
P LPS004 Lupus Erythematosus 61 0.069
189
VRL011 Viral Infectious Disease 61 0.069
190
MCL006 Macular Retinal Edema 55 0.069
191
LMB062 Limb Ischemia 55 0.069
192
c PST005 Posterior Uveitis 54 0.069
193
PRL017 Prolymphocytic Leukemia 47 0.069
194
PLS025 Plasmablastic Lymphoma 47 0.069
195
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.069
196
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.069
197
HDG004 Hodgkin's Granuloma 26 0.069
198
HDG006 Hodgkin's Paragranuloma 24 0.069
199
P BLD134 Bladder Cancer 78 0.066
200
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.066
201
c HPT073 Hepatitis C Virus 70 0.066
202
P PLM037 Pulmonary Hypertension 68 0.066
203
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.066
204
INT066 Interstitial Lung Disease 59 0.066
205
HPT046 Hepatic Veno-Occlusive Disease 56 0.066
206
P CRD246 Cardiovascular System Disease 56 0.066
207
P TRM003 Tremor 53 0.066
208
KRT006 Keratoconjunctivitis 53 0.066
209
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 52 0.066
210
P HML001 Hemolytic-Uremic Syndrome 52 0.066
211
SPL004 Splenic Marginal Zone Lymphoma 51 0.066
212
PTT041 Pituitary Stalk Interruption Syndrome 50 0.066
213
LNG031 Lung Benign Neoplasm 50 0.066
214
c CHR418 Chronic Leukemia 50 0.066
215
P OVR082 Overgrowth Syndrome 50 0.066
216
KRT001 Keratoconjunctivitis Sicca 50 0.066
217
ATY042 Atypical Chronic Myeloid Leukemia 49 0.066
218
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 48 0.066
219
c MCR120 Microvascular Complications of Diabetes 7 47 0.066
220
c MCR130 Microvascular Complications of Diabetes 6 41 0.066
221
c MCR133 Microvascular Complications of Diabetes 4 41 0.066
222
HMN035 Hemangioma-Thrombocytopenia Syndrome 41 0.066
223
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.066
224
c NRF024 Neurofibromatosis, Type I 71 0.063
225
P NRB001 Neuroblastoma 71 0.063
226
c FNC043 Fanconi Anemia, Complementation Group E 62 0.063
227
P CTR002 Cataract 60 0.063
228
P SZR006 Seizure Disorder 58 0.063
229
c INT064 Intermediate Uveitis 55 0.063
230
GLC003 Glucose Intolerance 54 0.063
231
ANG065 Angioma, Tufted 39 0.063
232
ATM052 Autoimmune Disease 1 37 0.063
233
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.063
234
LYM095 Lymphangiomatosis 33 0.063
235
P CLR023 Colorectal Cancer 98 0.059
236
P OVR042 Ovarian Cancer 89 0.059
237
STR067 Stroke, Ischemic 80 0.059
238
BRN028 Brain Cancer 73 0.059
239
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.059
240
CRB039 Cerebrovascular Disease 69 0.059
241
P RHB003 Rhabdomyosarcoma 62 0.059
242
P HML002 Hemolytic Anemia 62 0.059
243
SQM006 Squamous Cell Carcinoma 60 0.059
244
HRP004 Herpes Zoster 60 0.059
245
APH001 Aphthous Stomatitis 57 0.059
246
c ADL017 Adult T-Cell Leukemia 57 0.059
247
P INF037 Inflammatory Bowel Disease 56 0.059
248
HYP014 Hyperuricemia 51 0.059
249
CRY001 Cryptogenic Organizing Pneumonia 51 0.059
250
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.059
251
DBT006 Diabetic Macular Edema 48 0.059
252
P TCL004 T-Cell Leukemia 47 0.059
253
ACT003 Acute Kidney Tubular Necrosis 45 0.059
254
RDC006 Red Cell Aplasia 42 0.059
255
P PRP021 Peripheral Nervous System Neoplasm 39 0.059
256
P BRS047 Breast Cancer 96 0.056
257
IMM167 Immune Deficiency Disease 78 0.056
258
CRH001 Crohn's Disease 74 0.056
259
MYC006 Mycosis Fungoides 66 0.056
260
P ADN016 Adenocarcinoma 64 0.056
261
P PSR002 Psoriasis 62 0.056
262
P ANP001 Anaplastic Large Cell Lymphoma 61 0.056
263
P ENC018 Encephalopathy 61 0.056
264
PRT013 Portal Hypertension 60 0.056
265
SZR001 Sezary's Disease 60 0.056
266
VSL002 Visual Epilepsy 58 0.056
267
PMP006 Pemphigus Vulgaris, Familial 58 0.056
268
LYM027 Lymphopenia 57 0.056
269
P SJG008 Sjogren Syndrome 56 0.056
270
PNM008 Pneumothorax 56 0.056
271
P PMP001 Pemphigus 55 0.056
272
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.056
273
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.056
274
PST011 Pustulosis of Palm and Sole 52 0.056
275
SBP001 Subependymal Giant Cell Astrocytoma 48 0.056
276
CHR563 Chronic Eosinophilic Leukemia 48 0.056
277
P PRR002 Pure Red-Cell Aplasia 48 0.056
278
DRY001 Dry Eye Syndrome 47 0.056
279
CRD001 Cardiac Tamponade 46 0.056
280
KDN015 Kidney Angiomyolipoma 46 0.056
281
PRV003 Perivascular Epithelioid Cell Tumor 38 0.056
282
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.056
283
c PRS136 Prostate Cancer, Hereditary, 6 33 0.056
284
c PRS130 Prostate Cancer, Hereditary, 8 32 0.056
285
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.052
286
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.052
287
P ART005 Arteriovenous Malformation 65 0.052
288
MGK001 Megakaryocytic Leukemia 64 0.052
289
SKN016 Skin Disease 63 0.052
290
c ALP101 Alpha-Thalassemia 62 0.052
291
P VSC011 Vasculitis 62 0.052
292
P THL005 Thalassemia 60 0.052
293
THY029 Thyroid Carcinoma 59 0.052
294
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.052
295
PRP030 Purpura 55 0.052
296
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 55 0.052
297
P ANG015 Angioedema 54 0.052
298
PNM001 Pneumocystosis 54 0.052
299
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.052
300
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.052
301
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.052
302
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.052
303
c ACT134 Acute Liver Failure 51 0.052
304
P CHR345 Chronic Pain 50 0.052
305
HYL004 Hyaline Fibromatosis Syndrome 50 0.052
306
P CTN015 Cutaneous T Cell Lymphoma 49 0.052
307
47X002 47,xyy 49 0.052
308
PRS012 Pars Planitis 48 0.052
309
P NRV006 Nervous System Cancer 48 0.052
310
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.052
311
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.052
312
CRN017 Coronary Thrombosis 47 0.052
313
c CNT033 Central Nervous System Cancer 46 0.052
314
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.052
315
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.052
316
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.052
317
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.052
318
P OVR046 Ovarian Cyst 45 0.052
319
LYM051 Lymphomatoid Granulomatosis 45 0.052
320
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.052
321
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.052
322
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.052
323
NRF003 Neurofibrosarcoma 42 0.052
324
CHR286 Chronic Neutrophilic Leukemia 41 0.052
326
CYT004 Cytomegalic Inclusion Disease 31 0.052
327
P MDL005 Medulloblastoma 77 0.048
328
P RTN024 Retinoblastoma 72 0.048
329
c BTT014 Beta-Thalassemia 72 0.048
330
P SYS005 Systemic Scleroderma 70 0.048
331
P CHR012 Chronic Granulomatous Disease 67 0.048
332
PNC129 Pancreatic Adenocarcinoma 67 0.048
333
CHL065 Cholangiocarcinoma 67 0.048
334
FCT007 Factor Vii Deficiency 66 0.048
335
c MCR129 Microvascular Complications of Diabetes 1 66 0.048
336
P HRP006 Herpes Simplex 65 0.048
337
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 62 0.048
338
c ATM011 Autoimmune Hepatitis 62 0.048
339
c ANM038 Anemia, Autoimmune Hemolytic 61 0.048
340
AGN016 Aging 56 0.048
341
HPT022 Hepatoblastoma 56 0.048
342
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.048
343
HRY003 Hairy Cell Leukemia 55 0.048
344
P CYS039 Cystic Kidney Disease 54 0.048
345
PNC001 Pancytopenia 54 0.048
346
P RTN016 Retinal Degeneration 53 0.048
347
c FML008 Familial Retinoblastoma 53 0.048
348
PRP080 Peripheral Artery Disease 53 0.048
349
P PLM006 Pulmonary Alveolar Proteinosis 52 0.048
350
GNG012 Gingival Overgrowth 51 0.048
351
INT079 Intrahepatic Cholangiocarcinoma 50 0.048
352
c LRG017 Large Intestine Cancer 47 0.048
353
P HMN032 Human Herpesvirus 8 46 0.048
354
FBR054 Fibroma 44 0.048
355
c MCR112 Microvascular Complications of Diabetes 2 41 0.048
356
RFR002 Refractory Hairy Cell Leukemia 32 0.048
357
CYS041 Cystic Angiomatosis of Bone, Diffuse 28 0.048
358
CLS052 Classic Hairy Cell Leukemia 27 0.048
359
P RHM011 Rheumatoid Arthritis 80 0.044
360
c CWD006 Cowden Syndrome 1 77 0.044
361
HMN044 Human Immunodeficiency Virus Type 1 71 0.044
362
P ART022 Arthritis 70 0.044
363
c FML346 Familial Adenomatous Polyposis 1 70 0.044
364
MLN008 Melanoma 69 0.044
365
c BSL007 Basal Cell Carcinoma 68 0.044
366
SKN019 Skin Melanoma 67 0.044
367
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.044
368
P NSP012 Nasopharyngeal Carcinoma 67 0.044
369
FLL027 Fallopian Tube Carcinoma 67 0.044
370
P CWD010 Cowden Syndrome 66 0.044
371
P CCK001 Cockayne Syndrome 66 0.044
372
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.044
373
c WLM013 Wilms Tumor 1 65 0.044
374
P MYP004 Myopathy 64 0.044
375
RHB001 Rhabdoid Cancer 63 0.044
376
IDP011 Idiopathic Interstitial Pneumonia 63 0.044
377
P GLM045 Glioma 63 0.044
378
c WLM018 Wilms Tumor 5 62 0.044
379
P ESP024 Esophagitis 62 0.044
380
P PLM036 Pulmonary Fibrosis 61 0.044
381
P DRM010 Dermatomyositis 61 0.044
382
NTR005 Nutritional Deficiency Disease 61 0.044
383
P BNG030 Benign Ependymoma 60 0.044
384
PNM010 Pneumothorax, Primary Spontaneous 60 0.044
385
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.044
386
P BND020 Bone Disease 59 0.044
387
GST045 Gastroenteritis 59 0.044
388
GRD007 Grade Iii Astrocytoma 59 0.044
389
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.044
390
THY122 Thyroid Gland Cancer 58 0.044
391
CST005 Castleman Disease 57 0.044
392
P EPD003 Epidermolysis Bullosa Simplex 56 0.044
393
ERY051 Erythroleukemia, Familial 56 0.044
394
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.044
395
P LCH002 Lichen Planus 54 0.044
396
GLS001 Gliosarcoma 54 0.044
397
c LKM070 Leukemia, Acute Monocytic 53 0.044
398
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.044
399
P EPD016 Epidermolysis Bullosa 53 0.044
400
CLL010 Cellular Ependymoma 53 0.044
401
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.044
402
P CPL006 Capillary Hemangioma 51 0.044
403
HYP017 Hypophosphatemia 49 0.044
404
FDL002 Food Allergy 49 0.044
405
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.044
406
RFR010 Refractory Anemia 48 0.044
407
IGG001 Iga Glomerulonephritis 48 0.044
408
CYS002 Cystic Lymphangioma 47 0.044
409
RNL077 Renal Fibrosis 47 0.044
410
EVN001 Evans' Syndrome 46 0.044
411
MLT113 Multicentric Castleman Disease 46 0.044
412
GLL048 Glial Tumor 45 0.044
413
c MLG068 Malignant Glioma 45 0.044
414
c HYP272 Hypercholesterolemia, Familial, 3 43 0.044
415
RDN001 Reading Disorder 40 0.044
416
c OVR114 Ovarian Cancer 1 38 0.044
417
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.044
418
ASC009 Ascites, Chylous 36 0.044
419
PRG023 Progeroid Short Stature with Pigmented Nevi 33 0.044
420
c MYC058 Myocardial Infarction 2 28 0.044
421
CHL079 Children's Interstitial Lung Disease 27 0.044
422
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.044
423
DFF031 Diffuse Alveolar Hemorrhage 26 0.044
425
P GST053 Gastric Cancer 83 0.040
426
c FNC027 Fanconi Anemia, Complementation Group a 81 0.040
427
GST019 Gastrointestinal Stromal Tumor 76 0.040
428
SVR004 Severe Combined Immunodeficiency 73 0.040
429
c THR092 Thrombophilia Due to Thrombin Defect 73 0.040
430
P FML011 Familial Adenomatous Polyposis 72 0.040
431
P EPL164 Epilepsy 71 0.040
432
P DMN001 Diamond-Blackfan Anemia 69 0.040
433
ART016 Aortic Aneurysm 68 0.040
434
BRN024 Bronchitis 68 0.040
435
P INF038 Influenza 68 0.040
436
P OLG002 Oligodendroglioma 67 0.040
437
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.040
438
P LPS002 Liposarcoma 65 0.040
439
P ATS364 Autism 65 0.040
440
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.040
441
MSC007 Muscle Hypertrophy 63 0.040
442
INT002 Intermittent Claudication 61 0.040
443
DRM006 Dermatitis 61 0.040
444
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.040
445
c PCH015 Pachyonychia Congenita 1 60 0.040
446
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.040
447
CRD132 Cardiac Conduction Defect 59 0.040
448
c DWL002 Dowling-Degos Disease 1 58 0.040
449
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.040
450
PLY023 Polycystic Liver Disease 57 0.040
451
P CHN012 Chondrosarcoma 56 0.040
452
PHR003 Pharyngitis 56 0.040
453
ISL001 Islet Cell Tumor 56 0.040
454
BCT022 Bacterial Infectious Disease 56 0.040
455
CMR002 Coumarin Resistance 56 0.040
456
HMG005 Hemoglobinopathy 55 0.040
457
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.040
458
HMS001 Hemosiderosis 54 0.040
459
c ACT020 Acute T Cell Leukemia 53 0.040
460
GLS018 Glass Syndrome 53 0.040
461
CRH005 Crohn's Colitis 52 0.040
462
ERD001 Erdheim-Chester Disease 52 0.040
463
TLN003 Telangiectasis 51 0.040
464
MCR141 Mucormycosis 51 0.040
465
P FNC004 Fanconi Syndrome 50 0.040
466
IRD001 Iridocyclitis 50 0.040
467
c INF145 Infantile Liver Failure Syndrome 1 50 0.040
468
c MLG054 Malignant Histiocytosis 50 0.040
469
LFT001 Left Bundle Branch Hemiblock 49 0.040
470
HMG002 Hemoglobinuria 49 0.040
471
P SCL015 Scleritis 48 0.040
472
KRT013 Keratolytic Winter Erythema 46 0.040
473
CNG028 Congenital Hypoplastic Anemia 46 0.040
474
MXD026 Mixed Glioma 45 0.040
475
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.040
476
P BNG032 Benign Mesothelioma 45 0.040
477
CLL014 Cll/sll 45 0.040
478
PRT035 Peritoneum Cancer 44 0.040
479
FBR019 Fibromatosis 44 0.040
480
LTH001 Lethal Midline Granuloma 43 0.040
481
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.040
482
P RRT020 Rare Tumor 41 0.040
483
c WLM011 Wilms Tumor 6 37 0.040
484
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.040
485
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.040
486
c ANT023 Anterior Scleritis 30 0.040
487
CYS044 Cystic Disease of Lung 28 0.040
488
KPS005 Kaposiform Lymphangiomatosis 27 0.040
489
CYT018 Cytochrome P450 2d6 Variant 27 0.040
490
c ACQ016 Acquired Pure Red Cell Aplasia 26 0.040
491
c BKV001 Bk-Virus Nephropathy 23 0.040
492
P ATX030 Ataxia-Telangiectasia 83 0.034
493
MLR004 Malaria 80 0.034
494
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.034
495
ADR007 Adrenoleukodystrophy 74 0.034
496
END057 Endometrial Cancer 74 0.034
497
c ATR087 Atrial Standstill 1 74 0.034
498
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.034
499
LPT014 Leptin Deficiency or Dysfunction 73 0.034
500
BSL036 Basal Cell Nevus Syndrome 72 0.034
501
SCH036 Scheie Syndrome 71 0.034
502
MLT157 Multiple System Atrophy 1 70 0.034
503
P HYP086 Hypothyroidism 68 0.034
504
P MYC084 Mycobacterium Tuberculosis 1 68 0.034
505
c INF071 Inflammatory Bowel Disease 1 68 0.034
506
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 67 0.034
507
CMM004 Common Variable Immunodeficiency 67 0.034
508
LKC009 Leukocyte Adhesion Deficiency, Type I 67 0.034
509
CNN005 Connective Tissue Disease 66 0.034
510
MYX005 Myxoid Liposarcoma 66 0.034
511
SVR066 Severe Combined Immunodeficiency, X-Linked 65 0.034
512
AFB002 Afibrinogenemia, Congenital 65 0.034
513
GST092 Gastroesophageal Reflux 65 0.034
514
P THY023 Thymoma 65 0.034
515
DSM004 Desmoid Tumor 64 0.034
516
CLN015 Colon Adenocarcinoma 63 0.034
517
DPR016 Depression 63 0.034
518
c HPT003 Hepatitis a 63 0.034
519
c SCL052 Scleroderma, Familial Progressive 62 0.034
520
CLT003 Colitis 62 0.034
521
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.034
522
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.034
523
ACQ007 Acquired Immunodeficiency Syndrome 60 0.034
524
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.034
525
ORL011 Oral Cancer 60 0.034
526
CHC001 Chickenpox 60 0.034
527
MXD005 Mixed Connective Tissue Disease 59 0.034
528
c HPT016 Hepatitis B 59 0.034
529
IRN001 Iron Deficiency Anemia 58 0.034
530
ADN018 Adenoma 58 0.034
531
P INF032 Infertility 57 0.034
532
c MST023 Mesothelioma, Malignant 57 0.034
533
MNT002 Mental Depression 57 0.034
534
P NRP001 Neuropathy 56 0.034
535
PLS011 Plasmacytoma 56 0.034
536
P ALP008 Alopecia 56 0.034
537
GST050 Gastrointestinal System Disease 56 0.034
538
INT030 Intracranial Aneurysm 56 0.034
539
DFF005 Diffuse Large B-Cell Lymphoma 56 0.034
540
GRN034 Grange Syndrome 55 0.034
541
P PLY018 Polycythemia 55 0.034
542
JVN009 Juvenile Pilocytic Astrocytoma 55 0.034
543
NRN004 Neuroendocrine Tumor 55 0.034
544
PLM010 Pulmonary Edema 55 0.034
545
P ANT006 Antiphospholipid Syndrome 54 0.034
546
CLL003 Cellulitis 54 0.034
547
P ESP035 Esophagitis, Eosinophilic, 1 54 0.034
548
c THY107 Thymoma, Familial 54 0.034
549
ACD008 Acid-Labile Subunit Deficiency 54 0.034
550
PRP036 Peripheral T-Cell Lymphoma 53 0.034
551
P HST010 Histiocytosis 53 0.034
552
P RTN018 Retinal Disease 52 0.034
553
STR039 Sturge-Weber Syndrome 52 0.034
554
P INT068 Intestinal Disease 52 0.034
555
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.034
556
ESN005 Eosinophilic Gastroenteritis 52 0.034
557
CRT016 Carotid Artery Disease 52 0.034
558
GNT002 Giant Cell Glioblastoma 52 0.034
559
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 0.034
560
c PSR017 Psoriasis 2 52 0.034
561
P LCT001 Lactic Acidosis 51 0.034
562
THY030 Thyroid Gland Disease 51 0.034
563
DSM003 Desmoid Disease, Hereditary 50 0.034
564
FBR008 Fibrillary Astrocytoma 50 0.034
565
P MMB011 Membranous Nephropathy 50 0.034
566
PRT018 Portal Vein Thrombosis 50 0.034
567
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.034
568
P IGN003 Iga Nephropathy 1 49 0.034
569
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.034
570
c PSR023 Psoriasis 1 49 0.034
571
RTC005 Reticulosarcoma 49 0.034
572
GST049 Gastrointestinal System Cancer 49 0.034
573
BNR002 Bone Resorption Disease 48 0.034
574
c CNG208 Congenital Disorder of Glycosylation, Type Iic 48 0.034
575
KHN001 Kuhnt-Junius Degeneration 48 0.034
576
INT054 Intraocular Lymphoma 48 0.034
577
SPL018 Splenomegaly 48 0.034
578
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.034
579
c BSL024 Basal Cell Carcinoma 1 47 0.034
580
GRM005 Germ Cell Cancer 47 0.034
581
c FCL025 Focal Segmental Glomerulosclerosis 1 47 0.034
582
NDL013 Nodular Regenerative Hyperplasia 47 0.034
583
c PRM093 Premature Ovarian Failure 7 47 0.034
584
c MLG069 Malignant Hypertension 47 0.034
585
INT067 Interstitial Nephritis 46 0.034
586
CRN019 Coronary Artery Vasospasm 46 0.034
587
PLS016 Plasma Cell Leukemia 46 0.034
588
GST071 Gastrointestinal Carcinoma 45 0.034
589
ACN001 Acinar Cell Carcinoma 45 0.034
590
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 45 0.034
591
PLX002 Plexiform Neurofibroma 45 0.034
592
ACT029 Acute Interstitial Pneumonia 44 0.034
593
c CLR017 Clear Cell Sarcoma 44 0.034
594
ESN004 Eosinophilic Gastritis 44 0.034
595
INT253 Intestinal Benign Neoplasm 44 0.034
596
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.034
597
LMY003 Leiomyomatosis 43 0.034
598
P EPT020 Epithelioid Hemangioendothelioma 43 0.034
599
ANP009 Anaplastic Oligodendroglioma 43 0.034
600
BCK006 Back Pain 42 0.034
601
DFF003 Diffuse Scleroderma 42 0.034
602
MSN004 Mesenchymal Cell Neoplasm 41 0.034
603
P RRH023 Rare Hereditary Hemochromatosis 41 0.034
604
ACT088 Acute Insulin Response 41 0.034
605
LRG008 Large Granular Lymphocyte Leukemia 41 0.034
606
P MSN005 Mesenchymal Chondrosarcoma 40 0.034
607
PNC015 Pancreatic Acinar Cell Adenocarcinoma 40 0.034
608
RTR011 Retroperitoneal Fibrosis 40 0.034
609
CRB086 Cerebral Aneurysms 40 0.034
610
ULC007 Ulcerative Stomatitis 39 0.034
611
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.034
612
c PSR028 Psoriasis 7 39 0.034
613
c CHR682 Chronic Bilirubin Encephalopathy 38 0.034
614
c PSR032 Psoriasis 11 38 0.034
615
c PSR018 Psoriasis 13 38 0.034
616
c SYS043 Systemic Lupus Erythematosus 1 38 0.034
617
CPL002 Capillary Lymphangioma 38 0.034
618
FBR089 Fibrosclerosis, Multifocal 38 0.034
619
INT020 Intravenous Leiomyomatosis 36 0.034
620
c ADL008 Adult Oligodendroglioma 35 0.034
621
SML008 Small Intestine Lymphoma 35 0.034
622
RFR013 Refractory Celiac Disease 35 0.034
623
WBR001 Weber Syndrome 34 0.034
624
P MYX008 Myxoid Chondrosarcoma 32 0.034
625
P PLY188 Polyendocrinopathy 32 0.034
626
CHN019 Chand Syndrome 32 0.034
627
RFR004 Refractory Hematologic Cancer 30 0.034
628
ACN026 Acinar Cell Carcinoma of Pancreas 28 0.034
629
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 27 0.034
630
PLS031 Plastic Bronchitis 27 0.034
631
ACT118 Acute Non Lymphoblastic Leukemia 27 0.034
632
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 26 0.034
633
INT358 Intestinal Polyposis Syndrome 25 0.034
634
PLY179 Polyomavirus-Associated Nephropathy 23 0.034
635
DFF027 Diffuse Lymphatic Malformation 22 0.034
636
PRM324 Primary Eosinophilic Gastrointestinal Disease 18 0.034
637
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 17 0.034
638
ESP021 Esophageal Cancer 90 0.028
639
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.028
640
P LNG064 Lung Cancer Susceptibility 3 77 0.028
641
P MLT020 Multiple Sclerosis 72 0.028
642
APR006 Apert Syndrome 70 0.028
643
LGH007 Leigh Syndrome 70 0.028
644
PTZ001 Peutz-Jeghers Syndrome 69 0.028
645
PLY001 Polycythemia Vera 69 0.028
646
c MGR028 Migraine with or Without Aura 1 69 0.028
647
P ESS003 Essential Thrombocythemia 67 0.028
648
P CRD119 Cardiac Arrest 67 0.028
649
SVR097 Severe Cutaneous Adverse Reaction 67 0.028
650
c FML001 Familial Atrial Fibrillation 66 0.028
651
ALC007 Alcohol Dependence 66 0.028
652
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.028
653
P ASP006 Aspergillosis 66 0.028
654
P ATR011 Atrial Fibrillation 66 0.028
655
MRK001 Merkel Cell Carcinoma 66 0.028
656
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 0.028
657
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 64 0.028
658
P MTR014 Motor Neuron Disease 64 0.028
659
TBC004 Tobacco Addiction 64 0.028
660
P ADL010 Adult Respiratory Distress Syndrome 63 0.028
661
c ACT068 Acute Cystitis 63 0.028
662
ACT119 Acute Promyelocytic Leukemia 63 0.028
663
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.028
664
P LMY004 Leiomyosarcoma 62 0.028
665
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.028
666
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 0.028
667
c BRN108 Branchiootic Syndrome 1 61 0.028
668
c ORF037 Orofaciodigital Syndrome I 61 0.028
669
CHL068 Cholestasis 60 0.028
670
INS001 Insulinoma 60 0.028
671
P ALP009 Alopecia Areata 60 0.028
672
c ACT027 Acute Pancreatitis 59 0.028
673
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.028
674
P CYS018 Cystitis 59 0.028
675
PLM033 Pulmonary Embolism 59 0.028
676
LNG108 Langerhans Cell Histiocytosis 58 0.028
677
ANG020 Angiosarcoma 58 0.028
678
P URT039 Urticaria 58 0.028
679
c PRG126 Progressive Familial Heart Block 58 0.028
680
EXT034 Extrinsic Allergic Alveolitis 58 0.028
681
NWB001 Newborn Respiratory Distress Syndrome 58 0.028
682
PLM070 Pulmonic Stenosis 57 0.028
683
CNS004 Constipation 57 0.028
684
CNT047 Contact Dermatitis 57 0.028
685
ERY003 Erythema Multiforme 57 0.028
686
P HDC001 Headache 57 0.028
687
DSS008 Disease of Mental Health 57 0.028
688
P PRP019 Peripheral Nervous System Disease 57 0.028
689
TRN018 Transitional Cell Carcinoma 56 0.028
690
HYP266 Hypoxia 56 0.028
691
LMY014 Leiomyoma, Uterine 56 0.028
692
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.028
693
ALL010 Allergic Contact Dermatitis 55 0.028
694
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.028
695
TNG003 Tongue Cancer 55 0.028
696
HST011 Histoplasmosis 54 0.028
697
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 54 0.028
698
EPT010 Epithelial-Myoepithelial Carcinoma 53 0.028
699
RFL001 Reflex Sympathetic Dystrophy 53 0.028
700
P LTR001 Lateral Sclerosis 53 0.028
701
P SHR001 Short Bowel Syndrome 52 0.028
702
EXP004 Exophthalmos 52 0.028
703
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.028
704
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.028
705
PRG017 Paraganglioma and Gastric Stromal Sarcoma 52 0.028
706
P INS002 in Situ Carcinoma 52 0.028
707
IMP005 Impotence 52 0.028
708
DSM007 Desmoplastic Small Round Cell Tumor 52 0.028
709
TXC002 Toxic Encephalopathy 52 0.028
710
c PRM012 Primary Polycythemia 52 0.028
711
CYS036 Cystinosis, Nephropathic 51 0.028
712
ILS001 Ileus 51 0.028
713
ACT017 Acute Chest Syndrome 50 0.028
714
CLR003 Clear Cell Adenocarcinoma 50 0.028
715
P HYP077 Hypertrichosis 50 0.028
716
HPT014 Hepatorenal Syndrome 50 0.028
717
LMY002 Leiomyoma 50 0.028
718
NPH018 Nephrogenic Systemic Fibrosis 50 0.028
719
DYS073 Dysphagia 50 0.028
720
RSD004 Rosai-Dorfman Disease 50 0.028
721
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 49 0.028
722
PLM041 Pulmonary Valve Stenosis 49 0.028
723
MYL003 Myeloid Sarcoma 49 0.028
724
BHR001 Behr Syndrome 49 0.028
725
c THR090 Thrombocythemia 1 49 0.028
726
c INV001 Invasive Aspergillosis 48 0.028
727
SXL003 Sexual Disorder 48 0.028
728
P RNL015 Renal Hypertension 48 0.028
729
CMB081 Combined Immunodeficiency, X-Linked 48 0.028
730
HPR003 Heparin-Induced Thrombocytopenia 47 0.028
731
MDS022 Mediastinitis 47 0.028
732
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.028
733
ANR004 Anuria 46 0.028
734
P EPN001 Ependymoblastoma 45 0.028
735
INT304 Interstitial Pneumonitis, Desquamative, Familial 45 0.028
736
ORL013 Oral Lichen Planus 45 0.028
737
P LPM005 Lipomatosis 45 0.028
738
GRN017 Granulocytopenia 44 0.028
739
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.028
740
TRP009 Triple X Syndrome 42 0.028
741
MYF001 Myofibroma 42 0.028
742
c MLG079 Malignant Pleural Mesothelioma 42 0.028
743
GST020 Gastric Antral Vascular Ectasia 41 0.028
744
c CPL013 Capillary Malformations, Congenital 40 0.028
745
c CNG027 Congenital Hemolytic Anemia 40 0.028
746
CRY019 Cryohydrocytosis 40 0.028
747
PLM068 Pulmonary Vein Stenosis 40 0.028
748
BRN036 Brain Stem Infarction 39 0.028
749
ENT001 Enterocele 39 0.028
750
ALG001 Algoneurodystrophy 39 0.028
751
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.028
752
OVR094 Ovarian Epithelial Cancer 38 0.028
753
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.028
754
GRM010 Germ Cells Tumors 34 0.028
755
ANG062 Angioosteohypertrophic Syndrome 33 0.028
756
RNL001 Renal Artery Obstruction 33 0.028
757
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.028
758
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.028
759
c JVN034 Juvenile Polyposis of Infancy 31 0.028
760
VRT003 Vertebrobasilar Insufficiency 31 0.028
761
FNT004 Fainting 31 0.028
762
ENG004 Engraftment Syndrome 30 0.028
763
ERY066 Erythema Multiforme Major 28 0.028
764
TCH005 Tièche-Jadassohn Nevus 27 0.028
765
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.028
766
FTL073 Fetal Anticonvulsant Syndrome 26 0.028
767
BRT037 Brittle Diabetes 25 0.028
768
CHR208 Chromosome 17p Deletion 23 0.028
769
PRP101 Peripheral Pulmonary Stenosis 22 0.028
770
c CRN172 Coronary Heart Disease 3 19 0.028
771
c INF152 Infectious Posterior Uveitis 19 0.028
772
BND002 B- and T-Cell Mixed Leukemia 18 0.028
773
c NNN032 Non-Infectious Posterior Uveitis 18 0.028
774
P ALZ034 Alzheimer Disease 88 0.020
775
CYS001 Cystic Fibrosis 80 0.020
776
c DLT002 Dilated Cardiomyopathy 79 0.020
777
CNN003 Conn's Syndrome 79 0.020
778
P LYN001 Lynch Syndrome 77 0.020
779
AST005 Asthma 77 0.020
780
P PRK057 Parkinson Disease, Late-Onset 76 0.020
781
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.020
782
P SCH015 Schizophrenia 75 0.020
783
c MNN043 Meningioma, Familial 74 0.020
784
P OST002 Osteoporosis 73 0.020
785
VNH007 Von Hippel-Lindau Syndrome 73 0.020
786
ULC004 Ulcerative Colitis 73 0.020
787
ANX010 Anxiety 72 0.020
788
AGM019 Agammaglobulinemia, X-Linked 72 0.020
789
P PHC003 Pheochromocytoma 71 0.020
790
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.020
791
WLS001 Wilson Disease 70 0.020
792
ADN011 Adenoid Cystic Carcinoma 70 0.020
793
GST040 Gastric Adenocarcinoma 70 0.020
794
c GLY008 Glycogen Storage Disease Ii 70 0.020
795
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.020
796
RCK004 Rickets 69 0.020
797
P OCL013 Oculodentodigital Dysplasia 69 0.020
798
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 0.020
799
NVS017 Nevus, Epidermal 68 0.020
800
P MYS003 Myasthenia Gravis 68 0.020
801
c FML021 Familial Hypercholesterolemia 68 0.020
802
P JVN014 Juvenile Polyposis Syndrome 68 0.020
803
MST024 Mastocytosis, Cutaneous 67 0.020
804
P KBK002 Kabuki Syndrome 1 67 0.020
805
c ATS007 Autism Spectrum Disorder 67 0.020
806
P DMN002 Dementia 67 0.020
807
THY111 Thyroid Carcinoma, Familial Medullary 67 0.020
808
PSY004 Psychotic Disorder 67 0.020
809
STH001 Saethre-Chotzen Syndrome 67 0.020
810
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.020
811
P HYP061 Hypertrophic Cardiomyopathy 66 0.020
812
AND002 Androgen Insensitivity Syndrome 66 0.020
813
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.020
814
P HYP098 Hypereosinophilic Syndrome 66 0.020
815
P NRV007 Nervous System Disease 66 0.020
816
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.020
817
CRN036 Craniopharyngioma 65 0.020
818
P HYD006 Hydrocephalus 65 0.020
819
P CNJ013 Conjunctivitis 65 0.020
820
P AGM001 Agammaglobulinemia 65 0.020
821
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.020
822
RBR001 Roberts Syndrome 65 0.020
823
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.020
824
PRT036 Peritonitis 65 0.020
825
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.020
826
P PLR004 Pleuropulmonary Blastoma 65 0.020
827
BRR014 Barrett Esophagus 64 0.020
828
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.020
829
INC002 Inclusion Body Myositis 64 0.020
830
KWS002 Kawasaki Disease 64 0.020
831
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.020
832
KHL003 Kohlschutter-Tonz Syndrome 64 0.020
833
GT001 Gout 63 0.020
834
PRP083 Porphyria, Acute Intermittent 63 0.020
835
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.020
836
c SYS004 Systemic Mastocytosis 63 0.020
837
END041 Endometrial Adenocarcinoma 63 0.020
838
P MST009 Mastocytosis 63 0.020
839
THY121 Thyroid Gland Anaplastic Carcinoma 63 0.020
840
P ANR048 Aniridia 1 63 0.020
841
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.020
842
P HRD008 Hereditary Hemorrhagic Telangiectasia 62 0.020
843
P PRM002 Primary Hyperoxaluria 62 0.020
844
BRS099 Breast Ductal Carcinoma 62 0.020
845
P BCK002 Beckwith-Wiedemann Syndrome 62 0.020
846
P ART023 Arthropathy 62 0.020
847
PRM126 Primary Peritoneal Carcinoma 62 0.020
848
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.020
849
TRN015 Transient Cerebral Ischemia 62 0.020
850
MNN042 Meningioma, Radiation-Induced 62 0.020
851
PSR001 Psoriatic Arthritis 62 0.020
852
BRT002 Birt-Hogg-Dube Syndrome 62 0.020
853
P PRP029 Porphyria 62 0.020
854
BLD131 Bladder Urothelial Carcinoma 61 0.020
855
TKY002 Takayasu Arteritis 61 0.020
856
CRC021 Carcinosarcoma 61 0.020
857
ALV005 Alveolar Soft Part Sarcoma 61 0.020
858
OST003 Osteonecrosis 61 0.020
859
P PNC044 Pancreatitis 61 0.020
860
NRL005 Neurilemmoma 60 0.020
861
ACN002 Acanthosis Nigricans 60 0.020
862
HPT019 Hepatic Encephalopathy 60 0.020
863
P SLV026 Salivary Gland Carcinoma 60 0.020
864
CRD223 Cardiac Arrhythmia 60 0.020
865
CHR001 Churg-Strauss Syndrome 60 0.020
866
MRT001 Muir-Torre Syndrome 60 0.020
867
P SCL018 Scoliosis 60 0.020
868
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.020
869
FCL081 Focal Cortical Dysplasia, Type Ii 60 0.020
870
CHR072 Chordoma 59 0.020
871
P GLY013 Glycogen Storage Disease 59 0.020
872
P MYC008 Myocarditis 59 0.020
873
IMM174 Immunodeficiency with Hyper-Igm, Type 1 59 0.020
874
GNG013 Gingivitis 59 0.020
875
HYD002 Hydronephrosis 59 0.020
876
c LPM012 Lipomatosis, Multiple 59 0.020
877
FBR086 Fibrolamellar Carcinoma 59 0.020
878
c SVR003 Severe Congenital Neutropenia 59 0.020
879
HLC007 Helicobacter Pylori Infection 59 0.020
880
P HMN036 Hemangiopericytoma, Malignant 58 0.020
881
THY025 Thymus Cancer 58 0.020
882
c PRG043 Progressive Familial Heart Block, Type Ib 58 0.020
883
P ALC033 Alcohol Use Disorder 58 0.020
884
PST028 Post-Traumatic Stress Disorder 58 0.020
885
P MLN069 Melanoma, Uveal 58 0.020
886
BRS051 Breast Disease 58 0.020
887
c THY102 Thyroid Cancer, Nonmedullary, 2 57 0.020
888
P OPT006 Optic Nerve Disease 57 0.020
889
P PRV006 Pervasive Developmental Disorder 57 0.020
890
c PRG018 Paragangliomas 1 57 0.020
891
THY022 Thymic Carcinoma 57 0.020
892
EMB004 Embryonal Carcinoma 57 0.020
893
DSS009 Disseminated Intravascular Coagulation 57 0.020
894
BLR008 Bilirubin Metabolic Disorder 57 0.020
895
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.020
896
HMR039 Hemorrhage, Intracerebral 57 0.020
897
SRC027 Sarcoma, Synovial 56 0.020
898
P PYL005 Pyelonephritis 56 0.020
899
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 56 0.020
900
P FBR017 Fibrosarcoma 56 0.020
901
PGM001 Pigmented Villonodular Synovitis 56 0.020
902
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 56 0.020
903
ORL005 Oral Candidiasis 56 0.020
904
GLL018 Gallbladder Cancer 56 0.020
905
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 56 0.020
906
KRT071 Keratosis, Seborrheic 56 0.020
907
ACS001 Acoustic Neuroma 56 0.020
908
P PLY011 Polycystic Ovary Syndrome 56 0.020
909
P PLY019 Polyneuropathy 56 0.020
910
P MYS005 Myositis 56 0.020
911
SYN007 Synovitis 55 0.020
912
VGN017 Vaginal Cancer 55 0.020
913
BRN004 Brain Edema 55 0.020
914
ZLL002 Zollinger-Ellison Syndrome 55 0.020
915
c BCT007 Bacterial Meningitis 55 0.020
916
CPL003 Capillary Leak Syndrome 55 0.020
917
P HYP076 Hyperthyroidism 55 0.020
918
CRC006 Carcinoid Syndrome 55 0.020
919
P MLT074 Multiple Endocrine Neoplasia 55 0.020
920
ACT200 Acute Monoblastic Leukemia 55 0.020
921
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.020
922
DBT010 Diabetic Neuropathy 55 0.020
923
CLF004 Cleft Lip/palate 54 0.020
924
PPL022 Papilloma 54 0.020
925
P LRY044 Larynx Cancer 54 0.020
926
P LNG035 Lung Large Cell Carcinoma 54 0.020
927
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.020
928
AMN001 Amenorrhea 54 0.020
929
P MNC007 Monocytic Leukemia 54 0.020
930
CLL002 Collecting Duct Carcinoma 54 0.020
931
OCL022 Ocular Melanoma 53 0.020
932
CLR030 Clear Cell Renal Cell Carcinoma 53 0.020
933
HDR002 Hidradenitis Suppurativa 53 0.020
934
ALC009 Alcoholic Liver Cirrhosis 53 0.020
935
P RCT021 Rectum Cancer 53 0.020
936
P ART018 Aortic Valve Insufficiency 53 0.020
937
KRT009 Keratosis 53 0.020
938
P OVR049 Ovarian Disease 53 0.020
939
GST023 Gastric Ulcer 53 0.020
940
P EMB005 Embryonal Rhabdomyosarcoma 53 0.020
941
CLF001 Cleft Lip 53 0.020
942
IMM102 Immunodeficiency 14 53 0.020
943
P PRG013 Paraganglioma 52 0.020
944
P HMR003 Hemorrhagic Disease 52 0.020
945
P END047 Endophthalmitis 52 0.020
946
P SML001 Small Cell Carcinoma 52 0.020
947
GTR002 Goiter 52 0.020
948
TND005 Tendinitis 52 0.020
949
P ACT008 Actinic Keratosis 52 0.020
950
SRS001 Serous Cystadenocarcinoma 52 0.020
951
P MSC003 Muscular Atrophy 52 0.020
952
INV006 Inverted Papilloma 52 0.020
953
DFF036 Differentiated Thyroid Carcinoma 51 0.020
954
P BRN035 Brain Stem Glioma 51 0.020
955
c VRL010 Viral Hepatitis 51 0.020
956
CYS014 Cystadenocarcinoma 51 0.020
957
MCR088 Microscopic Polyangiitis 51 0.020
958
THY125 Thyroid Gland Medullary Carcinoma 51 0.020
959
BLD053 Blood Platelet Disease 51 0.020
960
THR004 Thrombocytosis 51 0.020
961
SMT003 Somatostatinoma 51 0.020
962
SPP010 Suppressor of Tumorigenicity 3 51 0.020
963
NRM004 Neuroma 51 0.020
964
GSG001 Gas Gangrene 50 0.020
965
AZS001 Azoospermia 50 0.020
966
HYP081 Hypolipoproteinemia 50 0.020
967
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.020
968
BRN014 Bronchopneumonia 50 0.020
969
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 50 0.020
970
CLR109 Colorectal Adenocarcinoma 50 0.020
971
P CHL066 Cholangitis 50 0.020
972
P MGR003 Migraine with Aura 50 0.020
973
VPM001 Vipoma 50 0.020
974
c CNG216 Congenital Hydrocephalus 50 0.020
975
FSC004 Fasciitis 50 0.020
976
HYP080 Hypogonadism 50 0.020
977
P PRT096 Peritoneal Mesothelioma 50 0.020
978
CRV040 Cervix Carcinoma 50 0.020
979
P RNL007 Renal Tubular Acidosis 50 0.020
980
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.020
981
MCP006 Mucoepidermoid Carcinoma 50 0.020
982
VRR004 Verrucous Carcinoma 49 0.020
983
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.020
984
NPH010 Nephrosclerosis 49 0.020
985
BLP005 Blepharitis 49 0.020
986
RNL011 Renal Osteodystrophy 49 0.020
987
LRN003 Learning Disability 49 0.020
988
PNN001 Panniculitis 49 0.020
989
VCC001 Vaccinia 49 0.020
990
c LRG001 Large Cell Carcinoma 49 0.020
991
HDR003 Hidradenitis 49 0.020
992
OLF005 Olfactory Neuroblastoma 49 0.020
993
ADN009 Adenosquamous Carcinoma 49 0.020
994
GYN001 Gynecomastia 49 0.020
995
URM002 Uremia 49 0.020
996
CLN045 Colonic Benign Neoplasm 49 0.020
997
BCT004 Bacteriuria 48 0.020
998
P LYM024 Lymphatic System Disease 48 0.020
999
MLT145 Multiple Enchondromatosis, Maffucci Type 48 0.020
1000
VTM033 Vitamin K Deficiency Bleeding 48 0.020
1001
P OBS001 Obstructive Jaundice 48 0.020
1002
c NPH049 Nephrotic Syndrome, Type 2 48 0.020
1003
P BRS053 Breast Fibroadenoma 48 0.020
1004
END062 Endometrial Hyperplasia 48 0.020
1005
ONC007 Oncocytoma 48 0.020
1006
ACT098 Acute Erythroid Leukemia 48 0.020
1007
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.020
1008
CRC014 Carcinoid Tumors, Intestinal 48 0.020
1009
ART004 Aortic Atherosclerosis 48 0.020
1010
ACT084 Acute Stress Disorder 48 0.020
1011
STM006 Stomach Disease 48 0.020
1012
GLC106 Glucocorticoid Resistance, Generalized 48 0.020
1013
ADR016 Adrenal Cortical Carcinoma 48 0.020
1014
ESN015 Eosinophilic Fasciitis 47 0.020
1015
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.020
1016
GNG008 Ganglioneuroblastoma 47 0.020
1017
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 47 0.020
1018
RGH001 Right Bundle Branch Block 47 0.020
1019
P CRV031 Cervical Adenocarcinoma 47 0.020
1020
PPL002 Papillary Carcinoma 47 0.020
1021
ATN005 Autonomic Dysfunction 47 0.020
1022
SPN021 Spinal Meningioma 47 0.020
1023
NRN001 Neuroendocrine Carcinoma 47 0.020
1024
c BCT013 Bacterial Pneumonia 47 0.020
1025
MCR018 Microcytic Anemia 47 0.020
1026
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.020
1027
PPL018 Papillary Adenocarcinoma 46 0.020
1028
HRD005 Hard Palate Cancer 46 0.020
1029
SRT004 Serotonin Syndrome 46 0.020
1030
P BLD051 Blood Coagulation Disease 46 0.020
1031
HST009 Histiocytoma 46 0.020
1032
TST014 Testicular Cancer 46 0.020
1033
ADR040 Adrenal Gland Pheochromocytoma 46 0.020
1034
URT010 Ureteral Obstruction 46 0.020
1035
CNN010 Connective Tissue Benign Neoplasm 46 0.020
1036
KRT008 Keratopathy 46 0.020
1037
ANP006 Anaplastic Ependymoma 46 0.020
1038
FLL008 Folliculitis 46 0.020
1039
PRT019 Protein-Losing Enteropathy 46 0.020
1040
MCS004 Mucosal Melanoma 46 0.020
1041
SBP004 Subependymoma 46 0.020
1042
AYM001 Ayme-Gripp Syndrome 46 0.020
1043
MCR037 Macroglossia 45 0.020
1044
P CHR573 Choroid Plexus Cancer 45 0.020
1045
GST030 Gastrinoma 45 0.020
1046
DDF001 Dedifferentiated Liposarcoma 45 0.020
1047
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.020
1048
URT051 Ureter, Cancer of 45 0.020
1049
MYX001 Myxopapillary Ependymoma 45 0.020
1050
P SBR004 Seborrheic Dermatitis 45 0.020
1051
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.020
1052
GLC036 Glucagonoma 45 0.020
1053
LRY029 Laryngomalacia 45 0.020
1054
PPL001 Papillary Adenoma 45 0.020
1055
SPR005 Superficial Basal Cell Carcinoma 45 0.020
1056
INT071 Intestinal Perforation 45 0.020
1057
TCL003 T Cell Deficiency 45 0.020
1058
OLG001 Oligospermia 45 0.020
1059
IMM136 Immune System Disease 45 0.020
1060
CHR008 Choroiditis 44 0.020
1061
c CRT081 Cortical Dysplasia, Complex, with Other Brain Malformations 7 44 0.020
1062
c ADL023 Adult Medulloblastoma 44 0.020
1063
END035 Endocrine Gland Cancer 44 0.020
1064
MLG065 Malignant Fibroxanthoma 44 0.020
1065
APP009 Appendix Adenocarcinoma 44 0.020
1066
P GNT008 Giant Cell Tumor 44 0.020
1067
JVN033 Juvenile Nasopharyngeal Angiofibroma 44 0.020
1068
THR012 Thoracic Cancer 44 0.020
1069
MCR225 Macrophage Activation Syndrome 44 0.020
1070
P TST026 Testicular Germ Cell Cancer 44 0.020
1071
P PHR004 Pharynx Cancer 44 0.020
1072
c ATM099 Autoimmune Uveitis 44 0.020
1073
GST027 Gastric Lymphoma 44 0.020
1074
c JVN003 Juvenile Xanthogranuloma 44 0.020
1075
c RHB023 Rhabdomyosarcoma, Embryonal, 1 43 0.020